Cerenovus, Inc.
465 devices · 3,094 adverse event reports · 20 deaths reported · 194 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- CEREBASE GS9090SDCatheter, Percutaneous, Neurovasculature1 recall2 deaths97 reports
- CEREPAKTM MDH1Device, Vascular, for Promoting Embolization1 recall72 reports
- GALAXY G3 GLM915020DEVICE, NEUROVASCULAR EMBOLIZATION1 recall44 reports
- GALAXY G3 GLM920060Device, Vascular, for Promoting Embolization89 reports
- CEREBASE GS9095SDCatheter, Percutaneous, Neurovasculature1 recall1 death33 reports
- GALAXY G3 GLM910030Device, Vascular, for Promoting Embolization79 reports
- GALAXY G3 GLM910040Device, Vascular, for Promoting Embolization77 reports
- GALAXY G3 GLM910020DEVICE, NEUROVASCULAR EMBOLIZATION67 reports
- CEREBASE GS9080SDCatheter, Percutaneous, Neurovasculature1 recall13 reports
- CEREPAK FREEFORM MCR091020Device, Vascular, for Promoting Embolization1 recall12 reports
- CEREPAK FREEFORM MCR092060Device, Vascular, for Promoting Embolization1 recall12 reports
- CEREPAK FREEFORM MCR091040Device, Vascular, for Promoting Embolization1 recall10 reports
- CEREPAK FREEFORM MCR092030Device, Vascular, for Promoting Embolization1 recall8 reports
- CEREPAK FREEFORM XCR120304Device, Vascular, for Promoting Embolization1 recall7 reports
- CEREPAK FREEFORM XCR120308Device, Vascular, for Promoting Embolization1 recall7 reports
- CEREPAK FREEFORM XCR120410Device, Vascular, for Promoting Embolization1 recall7 reports
- CEREPAK HELIFORM XHE120208DEVICE, NEUROVASCULAR EMBOLIZATION1 recall7 reports
- CEREPAK FREEFORM MCR091030Device, Vascular, for Promoting Embolization1 recall6 reports
- CEREPAK FREEFORM MCR091530Device, Vascular, for Promoting Embolization1 recall6 reports
- CEREPAK FREEFORM MCR092040Device, Vascular, for Promoting Embolization1 recall6 reports
- CEREPAK FREEFORM XCR120306Device, Vascular, for Promoting Embolization1 recall6 reports
- CEREPAK FREEFORM MCR091540Device, Vascular, for Promoting Embolization1 recall5 reports
- CEREPAK FREEFORM MCR093060Device, Vascular, for Promoting Embolization1 recall5 reports
- CEREPAK FREEFORM XCR120515DEVICE, NEUROVASCULAR EMBOLIZATION1 recall5 reports
- CEREPAK UNIFORM FCX100356Device, Vascular, for Promoting Embolization1 recall5 reports
- CEREPAK FREEFORM SCR120407Device, Vascular, for Promoting Embolization1 recall4 reports
- CEREPAK FREEFORM XCR120406DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK FREEFORM XCR120408DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK FREEFORM XCR123505DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK FREEFORM XCR123509DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK UNIFORM FCX100407Device, Vascular, for Promoting Embolization1 recall4 reports
- CEREPAK UNIFORM FCX100730DEVICE, NEUROVASCULAR EMBOLIZATION1 recall4 reports
- CEREPAK FREEFORM MCR091525DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM SCR120615Device, Vascular, for Promoting Embolization1 recall3 reports
- CEREPAK FREEFORM SCR120721DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM XCR120202DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM XCR120510DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK FREEFORM XCR122505DEVICE, NEUROVASCULAR EMBOLIZATION1 recall3 reports
- CEREPAK UNIFORM FCX100517Device, Vascular, for Promoting Embolization1 recall3 reports
- CEREPAK FREEFORM SCR120410DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK FREEFORM SCR120620DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK FREEFORM SCR121230Device, Vascular, for Promoting Embolization1 recall2 reports
- CEREPAK HELIFORM SHD180312DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK HELIFORM SHD180415Device, Vascular, for Promoting Embolization1 recall2 reports
- CEREPAK FREEFORM XCR122535DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 death2 reports
- CEREPAK FREEFORM XCR123575Device, Vascular, for Promoting Embolization1 recall2 reports
- CEREPAK HELIFORM XHE120204Device, Vascular, for Promoting Embolization1 recall2 reports
- CEREPAK HELIFORM XHE120206DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX100412DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX100509Device, Vascular, for Promoting Embolization1 recall2 reports
- CEREPAK UNIFORM FCX100626DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX100713DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX181846DEVICE, NEUROVASCULAR EMBOLIZATION1 recall2 reports
- CEREPAK UNIFORM FCX180714Device, Vascular, for Promoting Embolization1 recall2 reports
- CODMAN 80-1407NEUROSURGICAL PADDIE1 recall2 reports
- GALAXY G3 GLY120515DEVICE, NEUROVASCULAR EMBOLIZATION51 reports
- GALAXY G3 GLX120306DEVICE, NEUROVASCULAR EMBOLIZATION51 reports
- GALAXY G3 GLM915030Device, Vascular, for Promoting Embolization51 reports
- CEREPAK UNIFORM FCX182050DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM MCR091015Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK FREEFORM MCR092535Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK FREEFORM MCR092545Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK FREEFORM MCR092555DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM MCR093040DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120306DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120308Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK FREEFORM SCR120412DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120510DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120610DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR120715DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM SCR121030Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK HELIFORM SHD180520DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK HELIFORM SHD181445Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK FREEFORM XCR120610Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK FREEFORM XCR120620DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM XCR122525DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK UNIFORM FCX181017Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK UNIFORM FCX181118Device, Vascular, for Promoting Embolization1 recall1 report
- CEREPAK UNIFORM FCX181447DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK UNIFORM FCX180510DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CEREPAK FREEFORM MCR092020DEVICE, NEUROVASCULAR EMBOLIZATION1 recall1 report
- CODMAN 80-1399NEUROSURGICAL PADDIE1 recall1 report
- CODMAN 80-1403NEUROSURGICAL PADDIE1 recall1 report
- CODMAN 80-1408NEUROSURGICAL PADDIE1 recall1 report
- DURAFORM 80-1477USDURA SUBSTITUTE1 recall0 reports
- CEREPAK FREEFORM MCR091010DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM MCR091025DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM MCR091520DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM MCR093080DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120202DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120515DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120815DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120824DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR120925DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR122505Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK FREEFORM SCR122535DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR123509DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK FREEFORM SCR123575Device, Vascular, for Promoting Embolization1 recall0 reports
- CEREPAK HELIFORM SHD100154DEVICE, NEUROVASCULAR EMBOLIZATION1 recall0 reports
- CEREPAK HELIFORM SHD100208Device, Vascular, for Promoting Embolization1 recall0 reports